| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:111681053-111681296 | Rare:63; Clinvar (benign):7 | ||||
| chrX:111681552-111681692 | Rare:56 | ||||
| chrX:118346433-118346579 | Rare:36 | ||||
| chrX:118495759-118495873 | Rare:14 | ||||
| chrX:119236471-119236691 | Rare:61 | ||||
| chrX:119468208-119468506 | Common:3; Rare:98 | ||||
| chrX:119574364-119574739 | Common:1; Rare:76 | ||||
| chrX:119791543-119791978 | Common:2; Rare:114 | ||||
| chrX:119871638-119872012 | Common:2; Rare:80; Clinvar (benign):4 | ||||
| chrX:119943339-119943344 | Rare:2 | ||||
| chrX:119943603-119943852 | Rare:44 | ||||
| chrX:120469079-120469359 | Common:1; Rare:64; Clinvar:9; Clinvar (benign):7 | ||||
| chrX:120538611-120538730 | Rare:15 | ||||
| chrX:120559857-120560146 | Rare:48 | ||||
| chrX:120560636-120561120 | Rare:89 |